{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Brooklyn Park",
      "address_1": "7611 Northland Dr N",
      "reason_for_recall": "Medtronic is recalling select lots of DLP Femoral Arterial Cannula product due to recent reports in which the user had difficulty or was unable to connect the cannula to the perfusion circuit tubing.",
      "address_2": "",
      "product_quantity": "1304 devices",
      "code_info": "Model 57414 / Lot Numbers:   2014124994, 2015016150, 2015016729, 2015020381, 2015021484, and 201501C886.      Model 57417 / Lot Numbers:  2014125438, 2015016317, 2015016695, 2015020566, 2015021401, 2015030166, 2015030435, 2015030629, and 201503C101.        Model 57421 / Lot Numbers:  2015016410 and 2015017102.      Model 96017 / Lot Numbers:  2015021260 and 2015030499       Model 96021 / Lot Number:  2015021134.",
      "center_classification_date": "20150626",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of :  AK, AZ, CA, CO, IN, KS, LA, MN, MT, NM, NY, OH, OR, PA, TX, UT, and  WI., and to the countries of :  Belgium, Brazil, Canada, Colombia, Denmark, France, Germany, Greece, Hungary, India, Ireland, Italy, Korea, Morocco, Netherlands, Poland, Qatar, Russian Federation, Saudi Arabia, Slovakia, Spain, Switzerland, Turkey, and United Kingdom.",
      "state": "MN",
      "product_description": "Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Replacement Kit, Models 96017 and 96021.  Sterilized using Ethylene Oxide.    The cannula and dilator components are polyurethane and have tapered proximal tips to aid in diameter transition from the dilator.  The dilator components utilize tip indicator bands for minimum tip alignment of the component parts.  The cannula body is marked for depth insertion.  The components are designed to fit over each other to progressively dilate the vessel during insertion.  The dilator allows a 0.1-cm (0.038-in) guidewire to pass through it to aid in insertion.  A soft, tapered transition fitting terminates in a 0.95-cm (3/8-in) connection site or barbed  connector.",
      "report_date": "20150708",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Perfusion Systems",
      "recall_number": "Z-1914-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71517",
      "termination_date": "20160309",
      "more_code_info": "",
      "recall_initiation_date": "20150612",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}